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Most of the earlier nanotube junction models have been based on molecular dynamics (MD) simulations and heuristic methods which are either computationally expensive or impossible to model large 3D structures.
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Clinical trials that are based on molecular profiling, or which include one of the above standard regimens should be encouraged.
Diagnosis is based on molecular methods.
Its learning is based on molecular evolution.
DSC is based on molecular and nanometer-scale components.
Molecular manufacturing will be based on molecular machine systems able to manipulate and assemble molecular components to make larger products.
Mixing in the reactor is based on molecular diffusion.
This is based on molecular data, and this is why now they are classified into the genus Onychoprion.
The model is based on molecular theory or thermodynamics, together with empirical corrections.
Another impacting factor could also influence the binder remobilization and could be based on molecular distributions.
Our demonstration is based on molecular beam epitaxy growth of CdTe, MgTe, and ZnTe buffers on GaAs (100) substrate.
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